Canonical Allele Identifier: CA354048708
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413986T>C , CM000665.2:g.119413986T>C GRCh38
NC_000003.11:g.119132833T>C , CM000665.1:g.119132833T>C GRCh37
NC_000003.10:g.120615523T>C NCBI36
NG_007665.2:g.124614T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2057T>C MANE Select ENSP00000264245.4:p.Leu686Pro
ENST00000264245.8:c.2057T>C ENSP00000264245.4:p.Leu686Pro
NM_020754.3:c.2057T>C NP_065805.2:p.Leu686Pro
XM_005247671.3:c.1964T>C XP_005247728.1:p.Leu655Pro
XM_006713714.2:c.1997T>C XP_006713777.1:p.Leu666Pro
XM_006713714.3:c.1997T>C XP_006713777.1:p.Leu666Pro
XM_017006955.1:c.1565T>C XP_016862444.1:p.Leu522Pro
NM_020754.4:c.2057T>C MANE Select NP_065805.2:p.Leu686Pro